Ester pre-extended epoxy-terminated viscosifiers and method for producing the same

ABSTRACT

Viscosifiers, especially terminated polymers that have functional terminal groups, the polymers being pre-extended by polyols and being reacted to give polymers that are terminated by other functional groups, are produced. The viscosifiers have a low content in educts or educt descendants that deteriorate the properties of compositions. The formation of high-molecular addition products is considerably reduced or even excluded so that the products obtained have low viscosity and good storage stability. The epoxy-terminated polymer of formula (I) is especially preferred.

TECHNICAL FIELD

The invention relates to the field of toughness improvers.

STATE OF THE ART

Polymers have been used as materials for some time. Some polymers, however, have the problem that the polymer matrix fractures on abrupt impact stress, i.e. their toughness is low. Especially polymer matrices based on epoxy resins are very firm but in many cases not very impact-resistant. There have therefore long been attempts to improve the impact resistance.

This has been attempted for some time now, for example, with the use of specific copolymers, which are referred to as so-called liquid rubbers. By virtue of the use of chemically reactive groups, such as hydroxyl, carboxyl, vinyl or amino groups, such liquid rubbers can be incorporated chemically into the matrix. For example, there have for some time existed reactive liquid rubbers butadiene/acrylonitrile copolymers terminated by hydroxyl, carboxyl, vinyl or amino groups, which are supplied by B.F. Goodrich, or Noveon, under the Hycaro® trade name. The starting basis used therefor is always the carboxyl-terminated butadiene/acrylonitrile copolymer, to which a large excess of a diamine, diepoxide or a glycidyl (meth)acrylate is typically added. However, this leads to the effect that, on the one hand, a high viscosity forms or, on the other hand, that a very high content of unconverted diamine, diepoxide or glycidyl (meth)acrylate, which either has to be removed in a complex manner or else significantly adversely affects the mechanical properties.

However, the desire in many cases is to obtain even further-enhanced impact resistance and to have a wider variety of toughness improvers. One such possibility in this direction consists in the chain extension of epoxy-terminated polymers by bisphenols or by the use of higher molecular weight epoxy resins in the preparation. Here too, according to the reaction regime, large amounts of unconverted bisphenols or of extended epoxy resins arise, both of which can quickly adversely affect the properties of compositions. Moreover, such adducts are rapidly no longer fluid, as a result of which compositions comprising such toughness improvers consequently can no longer be applied in a reliable process in many cases. In addition, the use of bisphenols leads to reduced storage stability.

SUMMARY OF THE INVENTION

It is therefore an object of the present invention to provide toughness improvers with functional end groups which are capable of alleviating the problems of the prior art. The polymers as claimed in claims 1, 9, 11 and 12 provide such polymers. They can all be prepared from a carboxyl-terminated polymer as claimed in claim 9, which in turn can be obtained from a readily obtainable carboxyl-terminated butadiene/acrylonitrile copolymer. The possibilities which arise from the different molecules for pre-extension and termination make possible a wide range of different toughness improvers, and allow tailoring to the requirements. The polymers terminated with functional groups have the great advantage that they have a narrow molecular weight distribution and a very high proportion of molecules suitable as toughness improvers.

This advantage arises especially through the process for preparing the carboxyl-terminated polymer as claimed in claim 9, which serves as a starting point for the preparation of the polymers as claimed in claims 1, 11 and 12, and especially through the process comprising two steps for preparing an end group-terminated polymer as claimed in claim 15. This process as claimed in claim 13 ensures that any unconverted reactants present are only substances which already act as toughness improvers, which likewise react to give reactive toughness improvers in any reaction step leading further to polymer as claimed in claim 1, 11 or 12. Therefore, only insignificant amounts, if any, of compounds which adversely affect the mechanical properties are formed, such that exceptionally potent toughness improvers can be provided. In spite of the many possibilities which arise from pre-extension and epoxy termination, the polymers have an astonishingly low viscosity.

The polymers as claimed in claims 1, 9, 11 and 12 can be used widely as means of increasing the impact resistance of a polymer matrix as claimed in claim 16. Particular preference is given to the use thereof in epoxy resin matrix.

Further aspects of the invention relate to compositions comprising polymers as claimed in claim 1, 9, 11 or 12, and to cured compositions as claimed in claims 22 and 23.

Particular preference is given to using such polymers in adhesives, especially heat-curing epoxy resin adhesives. They have exceptionally good impact resistances.

Preferred embodiments of the invention are the subject-matter of the dependent claims.

WAYS OF PERFORMING THE INVENTION

In a first aspect, the present invention relates to epoxy-terminated polymer of the formula (I).

In this formula, R¹ is a divalent radical of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN after removal of the terminal carboxyl groups. In addition, R² is a radical of a polyol which has n OH groups, after removal of n OH groups. In addition, Y¹ is H or methyl. R³ is a diglycidyl ether DGE after removal of the two glycidyl ether groups. Finally, n is 2 to 4, especially 2.

In this context, “glycidyl ether group” is understood to mean the group of the formula

i.e., as well as the case in which Y¹ in this formula is H, for the sake of simplicity in the present document, this also refers to that group of the latter formula in which Y¹ is methyl.

More particularly, R¹ is a radical as obtained by formal removal of the carboxyl groups of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN sold commercially under the Hycar® CTBN name by Noveon. It preferably has a structure of the formula (IV).

In this formula, the broken lines represent the attachment sites of the two carboxyl groups. R is a linear or branched alkylene radical having 1 to 6 carbon atoms, especially having 4 carbon atoms, which is optionally substituted by unsaturated groups. In an embodiment of which particular mention should be made, the substituent R is a substituent of the formula (VII), where the broken line here too represents the attachment sites.

In addition, the index q is from 40 to 100, especially from 50 to 90. In addition, the labels b and c represent the structural elements which originate from butadiene, and a represents the structural element which originates from acrylonitrile. The indices x, m and p in turn represent values which describe the ratio of the structural elements a, b and c relative to one another. The index x represents values of 0.05-0.3, the index m values of 0.5-0.8, the index p values of 0.1-0.2, with the proviso that the sum of x, m and p is equal to 1.

It is clear to the person skilled in the art that the structures shown in formula (IV), and also the further structures shown in formulae (V), (V′″) and (V′″), should be understood as simplified representations. The units a, b and c, or d and e or d′ and e′, may thus each be arranged randomly, alternately or blockwise with respect to one another. More particularly, formula (IV) is thus not necessarily a triblock copolymer.

The R² radical is a polyol P which has n OH groups, after removal of n OH groups.

Suitable polyols are especially the following polyols:

-   -   polyoxyalkylenepolyols, also known as polyetherpolyols, which         are the polymerization products of ethylene oxide, 1,2-propylene         oxide, 1,2- or 2,3-butylene oxide, tetrahydrofuran or mixtures         thereof, optionally polymerized with the aid of a starter         molecule having two or three active hydrogen atoms, for example         water, or compounds having two or three OH groups. It is         possible to use either polyoxyalkylenepolyols which have a low         degree of unsaturation (measured to ASTM D-2849-69 and reported         in milliequivalents of unsaturation per gram of polyol (meq/g)),         prepared, for example, with the aid of so-called double metal         cyanide complex catalysts (DMC catalysts for short), or         polyoxyalkylenepolyols with a higher degree of unsaturation,         prepared, for example, with the aid of anionic catalysts such as         NaOH, KOH or alkali metal alkoxides. Particularly suitable         substances are polyoxypropylenediols and -triols with a degree         of unsaturation lower than 0.02 meq/g and with a molecular         weight in the range of 300-20 000 daltons, polyoxybutylenediols         and -triols, polyoxypropylenediols and -triols with a molecular         weight of 400-8000 daltons, and so-called “EO-endcapped”         (ethylene oxide-endcapped) polyoxypropylenediols or -triols. The         latter are specific polyoxypropylenepolyoxyethylenepolyols which         are obtained, for example, by alkoxylating pure         polyoxypropylenepolyols with ethylene oxide on completion of the         polypropoxylation, and which thus have primary hydroxyl groups;     -   hydroxyl-terminated polybutadienepolyols, for example those         which are prepared by polymerizing 1,3-butadiene and allyl         alcohol or by oxidizing polybutadiene, and the hydrogenation         products thereof;     -   styrene-acrylonitrile-grafted polyetherpolyols, as supplied, for         example, by Elastogran under the Lupranol® name;     -   polyesterpolyols, prepared, for example, from di- to trihydric         alcohols, for example 1,2-ethanediol, diethylene glycol,         1,2-propanediol, dipropylene glycol, 1,4-butanediol,         1,5-pentanediol, 1,6-hexanediol, neopentyl glycol, glycerol,         1,1,1-trimethylolpropane or mixtures of the aforementioned         alcohols with organic dicarboxylic acids or the anhydrides or         esters thereof, for example succinic acid, glutaric acid, adipic         acid, suberic acid, sebacic acid, dodecanedicarboxylic acid,         maleic acid, fumaric acid, phthalic acid, isophthalic acid,         terephthalic acid and hexahydrophthalic acid, or mixtures of the         aforementioned acids, and polyesterpolyols formed from lactones,         for example ε-caprolactone;     -   polycarbonatepolyols, as obtainable by reacting, for example,         the abovementioned alcohols used to form the polyesterpolyols         with dialkyl carbonates, diaryl carbonates or phosgene;     -   1,2-ethanediol, diethylene glycol, 1,2-propanediol, dipropylene         glycol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol,         1,7-heptanediol, octane-diol, nonanediol, decanediol, neopentyl         glycol, pentaerythritol         (=2,2-bis-(hydroxymethyl)-1,3-propanediol), dipentaerythritol         (=3-(3-hydroxy-2,2-bishydroxymethylpropoxy)-2,2-bishydroxymethylpropan-1-ol),         glycerol (=1,2,3-propanetriol), trimethylolpropane         (=2-ethyl-2-(hydroxymethyl)-1,3-propanediol), trimethylolethane         (=2-(hydroxymethyl)-2-methyl-1,3-propanediol),         di(trimethylolpropane)         (=3-(2,2-bis(hydroxymethyl)butoxy)-2-ethyl-2-hydroxymethylpropan-1-ol),         di(trimethylolethane)         (=3-(3-hydroxy-2-hydroxymethyl-2-methylpropoxy)-2-hydroxymethyl-2-methylpropan-1-ol),         diglycerol (=bis(2,3-dihydroxypropyl)ether;     -   polyols as contained by reduction of dimerized fatty acids.

Diols have been found to be especially suitable polyols

Especially suitable polyols are polyoxyalkylenediols, especially of the formula (V).

In this formula, g′ is the structural element which originates from ethylene oxide, h′ is the structural element which originates from propylene oxide and i′ is the structural element which originates from tetrahydrofuran. In addition, g, h and i are each 0 to 40, with the proviso that the sum of g, h and i is ≧1.

These are especially (poly)ethylene glycols, (poly)propylene glycols, (poly)ethylene glycol/propylene glycols, or (poly)butylene glycol or poly(oxy-1,4-butanediyl)-α-hydro-ω-hydroxyl, which is known to the person skilled in the art as poly-THF or polytetramethylene ether glycol. Such polybutylene glycols are commercially available as product series under the Terathane® name from DuPont or the Poly-THF® name from BASF Corp.

The R³ radical is a diglycidyl ether DGE after removal of the two glycidyl ether groups.

In one embodiment, the diglycidyl ether DGE is an aliphatic or cycloaliphatic diglycidyl ether, especially a diglycidyl ether of difunctional saturated or unsaturated, branched or unbranched, cyclic or open-chain C₂-C₃₀ alcohols, e.g. ethylene glycol diglycidyl ether, butanediol diglycidyl ether, hexanediol diglycidyl ether, octanediol diglycidyl ether, cyclohexanedimethanol diglycidyl ether, neopentyl glycol diglycidyl ether.

More particularly, the diglycidyl ether DGE is firstly an aliphatic or cycloaliphatic diglycidyl ether, especially a diglycidyl ether of the formula (VI″) or (VI′″).

In these formulae, r is 1 to 9, especially 3 or 5. In addition, q is 0 to 10 and t is 0 to 10, with the proviso that the sum of q and t is ≧1. Finally, d is the structural element which originates from ethylene oxide, and e is the structural element which originates from propylene oxide. Formula (VI′″) is thus (poly)ethylene glycol diglycidyl ether, (poly)propylene glycol diglycidyl ether and (poly)ethylene glycol/propylene glycol diglycidyl ether, where the units d and e may be arranged in blocks, alternately or randomly.

Particularly suitable aliphatic or cycloaliphatic diglycidyl ethers are ethylene glycol diglycidyl ether, butanediol diglycidyl ether or hexanediol diglycidyl ether.

In a further embodiment, the diglycidyl ether DGE is an epoxy resin. The epoxy resin may be a liquid epoxy resin or a solid epoxy resin.

The term “solid epoxy resin” is very well known to the person skilled in the art of epoxides and is used in contrast to “liquid epoxy resins”. The glass transition temperature of solid resins is above room temperature, i.e. they can be comminuted to free-flowing powders at room temperature.

Preferred solid epoxy resins have the formula (VIII).

In this formula, the substituents R⁴, R⁵ and Y² are each independently H or CH₃. In addition, the index S1 is >1.5, especially 2 to 12.

In this document, the use of the term “independently” in connection with substituents, radicals or groups should be interpreted such that substituents, radicals or groups with the same designation may occur simultaneously in the same molecule with different definitions.

Such solid epoxy resins are commercially available, for example from Dow, Huntsman or Hexion.

Compounds of the formula (VIII) with an index S1 between 1 and 1.5 are referred to by the person skilled in the art as semisolid epoxy resins. For this present invention, they are likewise considered to be solid resins. However, preferred solid epoxy resins are solid epoxy resins in the narrower sense, i.e. the index S1 has a value of >1.5.

Preferred liquid epoxy resins have the formula (IX).

In this formula, the substituents R⁴, R⁵ and Y² are each independently H or CH₃. In addition, the index S1 has a value of 0 to 1. S1 preferably has a value of less than 0.2.

These are thus preferably diglycidyl ethers of bisphenol A (DGEBA), of bisphenol F and of bisphenol A/F (the designation “A/F” refers here to a mixture of acetone with formaldehyde which is used as the reactant in the preparation thereof). Such liquid resins are available, for example, as Araldite® GY 250, Araldite® PY 304, Araldite® GY 282 (Huntsman) or D.E.R.™ 331 or D.E.R.™ 330 (Dow) or Epikote 828 (Hexion).

In addition, the diglycidyl ether DGE may be an epoxidized Novolac.

In a further particularly preferred embodiment, the diglycidyl ether DGE is a diglycidyl ether which, after removal of the two glycidyl ether groups corresponding to the R³ radical, has the formula (VI) or (VI′).

In these formulae, R′, R″ and R′″ are each independently H, methyl or ethyl, z is 0 or 1 and s is 0 or 0.1-12.

A particularly preferred diglycidyl ether DGE is bisphenol F diglycidyl ether.

The epoxy-terminated polymer of the formula (I) can be prepared as follows:

In a first step (“pre-extension”), a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN of the formula HOOC—R¹—COOH and a polyol P of the formula R²(OH)_(n) are used in a stoichiometric ratio (n′≧n) of the HOOC—R¹—COOH to prepare a carboxyl-terminated polymer of the formula (I):

For this reaction, polyol P and HOOC—R¹⁻COOH are used in an amount such that the stoichiometric ratio of the COOH groups to OH groups [COOH]/[OH] is ≧2.

When this ratio=2, corresponding to n′=n, the trend is toward an increased proportion of higher molecular weight species, which can lead to significantly increased viscosities in the carboxyl-terminated polymer of the formula (II), or in the epoxy-terminated polymer of the formula (I), which can cause problems under some circumstances. At a ratio of <2 (corresponding to n′<n), especially of <<2, this problem is very significantly enhanced. Therefore, a value of >2 is preferred for this ratio. Typically, a value of >4, in particular >>2, corresponding to n′>>n, is very preferred. In these cases, the reaction mixture has a relatively high content of unconverted HOOC—R¹—COOH. However, this does not cause any further problems, as discussed below.

It is clear to the person skilled in the art that it is also possible to use mixtures of polyols P and/or carboxyl-terminated butadiene/acrylonitrile copolymers CTBN of the formula HOOC—R¹—COOH.

In a second step (“termination”), the carboxyl-terminated polymer of the formula (II) and a diglycidyl ether DGE of the formula (III) are used in a stoichiometric excess (n″≧n) of the diglycidyl ether DGE to prepare an epoxy-terminated polymer of the formula (I):

For this reaction, the polymer of the formula (II) and the diglycidyl ether of the formula (III) are used in such amounts relative to one another that the stoichiometric ratio of the glycidyl ether groups to COOH groups

is ≧2.

When this ratio=2, corresponding to n″=n, the proportion of higher molecular weight species is increased, which can lead to significantly increased viscosities in the epoxy-terminated polymer of the formula (I), which can cause problems under some circumstances. At a ratio of <2 (corresponding to n′<n), especially of <<2, this problem is very greatly enhanced. Therefore, preference is given to a value of >2 for this ratio. Typically, a value of >4, in particular >>2, corresponding to n″>>n, is very preferred.

If unconverted carboxyl-terminated butadiene/acrylonitrile copolymer CTBN HOOC—R¹⁻COOH from the first step is still present in the reactant mixture at the start of this second step, it is reacted in the second step to give an epoxy-terminated polymer of the formula (X) known from the prior art.

In this manner, it can be ensured that a maximum number of epoxy-terminated polymers which can be used as impact modifiers are present in the final mixture. More particularly, in contrast to the prior art process, the presence of a large molecular weight distribution is prevented, which leads to a deterioration in the application properties, especially a high viscosity.

It is clear to the person skilled in the art that it is also possible to use mixtures of carboxyl-terminated polymers of the formula (II) and/or diglycidyl ethers DGE of the formula (III). In such a mode of preparation, mixtures of epoxy-terminated polymers of the formula (I) form in situ.

In both steps, an ester is formed.

Such reactions of alcohol with carboxylic acids are known to those skilled in the art, as are the reaction conditions therefor. More particularly, this reaction can be effected at elevated temperature and optionally under the influence of catalysts.

The esterification of a polyol with the carboxyl-terminated butadiene/acrylonitrile copolymer CTBN is effected preferably at elevated temperature and especially under the influence of an esterification catalyst, especially of an acid. Such an acid is preferably sulfuric acid, p-toluenesulfonic acid, benzenesulfonic acid, methanesulfonic acid, phosphoric acid or phosphorous acid. Preference is given to sulfuric acid. The water formed in the esterification can be removed from the reaction mixture under atmospheric pressure or else under reduced pressure. It is also possible to conduct a gas stream over or through the reaction mixture. The gas stream used may, for example, be air or nitrogen.

The esterification of the diglycidyl ether DGE with the carboxyl-terminated polymer is effected preferably at elevated temperature, typically at temperatures of 100° C., preferably around 140° C., and optionally using catalysts and preferably under protective gas. Examples of such catalysts are triphenylphosphine, tertiary amines, quaternary phosphonium salts or quaternary ammonium salts.

Carboxyl-terminated polymers of the formula (II) thus form a further aspect of the present invention. The definition, options and preferred embodiments of the radicals and indices shown in this formula (II) correspond to those as have already been described above in detail for epoxy-terminated polymer of the formula (I).

A further aspect of the present invention is a process for preparing a carboxyl-terminated polymer of the formula (II) by a reaction of a polyol P of the formula R²(OH)_(n) with a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN of the formula HOOC—R¹—COOH, characterized in that R²(OH)_(n) and HOOC—R¹—COOH are used for this reaction in an amount relative to one another which corresponds to a stoichiometric ratio of the COOH groups to OH groups [COOH]/[OH] of ≧2. This process has already been described in detail above in this document.

A further aspect of the present invention is a process for preparing an epoxy-terminated polymer of the formula (I) by the reaction of a carboxyl-terminated polymer of the formula (II) with a diglycidyl ether DGE of the formula (III), characterized in that the polymer of the formula (II) and the diglycidyl ether of the formula (III) are used for this reaction in an amount relative to one another which corresponds to a stoichiometric ratio of the glycidyl ether groups to COOH groups

of ≧2.

This process has already been described in detail above in this document.

It is clear to the person skilled in the art that the epoxy-terminated polymers of the formula (I) can be reacted further. For instance, more particularly, extension by means of polyphenols, especially by means of bisphenols, such as bisphenol A, is very helpful under some circumstances in order to obtain even higher molecular weight epoxy-terminated polymers or phenol-terminated polymers, as represented, for example, in the following formulae (XIII) and (XIV):

In these formulae, the index f is 0 or 1. R⁹ here is H or an alkyl or alkenyl radical, especially an allyl radical.

Further aspects are reaction products formed from the carboxyl-terminated polymer of the formula (II) with diamines or (meth)acrylate-functional alcohols or glycidyl ether-functional (meth)acrylates, which lead especially to amine-terminated polymers of the formulae (XI), (XI′) and (XI″), or to (meth)acrylate-terminated polymers of the formulae (XII) and (XII′), according to the following illustrative reaction scheme:

In these formulae, R⁷ is H or methyl and R⁸ is a divalent radical, especially an alkylene, cycloalkylene or (poly)oxyalkylene radical. The diamines 1-(2-aminoethyl)piperazine (DA1) or 2-methylpentamethylenediamine (DA2) or 1,2-diaminocyclohexane (DA3), and the glycidyl (meth)acrylate (GMA) and the hydroxy-functional (meth)acrylate (HMA), are each used in a stoichiometric excess, i.e. k, k′, k″, k′″ and k″″ are each greater than n.

The reaction conditions for formation of amides and esters are known from the literature and can be applied to the synthesis of these reaction products, especially the polymers of the formula (XI), (XI′), (XI″), (XII) and (XII′).

A further aspect of the present invention is thus a process for preparing an end group-terminated polymer of the formula (XV),

comprising the following two steps:

-   -   a) pre-extension, i.e. reaction of a polyol of the formula         R²(OH)_(n) with a stoichiometric excess of a carboxyl-terminated         butadiene/acrylonitrile copolymer CTBN of the formula         HOOC—R¹—COOH to give a carboxyl-terminated polymer of the         formula (II) as already described above, in such a way that the         polyol P and HOOC—R¹—COOH are used in an amount relative to one         another such that the ratio of COOH groups to OH groups         [COOH]/[OH] is ≧2;         -   where the polyol P and the carboxyl-terminated             butadiene/acrylonitrile copolymer CTBN of the formula             HOOC—R¹—COOH should be selected as already described above;     -   b) termination, i.e. reacting a carboxyl-terminated polymer of         the formula (II) with a diglycidyl ether or with a diamine or         with a (meth)acrylate-functional alcohol or with a glycidyl         ether-functional (meth)acrylate in such a way that the         diglycidyl ether or the diamine or the (meth)acrylate-functional         alcohol or the glycidyl ether-functional (meth)acrylate and the         carboxyl-terminated polymer of the formula (II) are used in an         amount relative to one another which corresponds to one molecule         of diglycidyl ether or diamine or (meth)acrylate-functional         alcohol or glycidyl ether-functional (meth)acrylate per COOH         group of a molecule of carboxyl-terminated polymer of the         formula (II).

In formula (XV) here, R¹⁰ is a divalent radical and Q¹ is an end group which is selected from the group consisting of the formulae (XVI), (XVI′), (XVI″) and —NH₂.

with the proviso that

-   -   Q is —NH— in the case         -   in which Q¹ is —NH₂ or the formula (XVI″), and     -   Q is —O— or the formula (XVII) in the case         -   in which Q¹ is the formula (XVI′), and     -   Q is the formula (XVII) in the case         -   in which Q¹ is the formula (XVI).

End group-terminated polymers of the formula (XV) are considered to be especially the above-described epoxy-terminated polymers of the formula (I), carboxyl-terminated polymers of the formula (II), amine-terminated polymers of the formula (XI), (XI′) or (XI″) and (meth)acrylate-terminated polymers of the formula (XII) or (XII′).

The carboxyl-terminated polymers of the formula (II) thus prepared and end group-terminated polymers of the formula (XV) described, especially the epoxy-terminated polymers of the formula (I), amine-terminated polymers of the formula (XI), (XI′) or (XI″) and (meth)acrylate-terminated polymers of the formula (XII) or (XII′), can be used as a means of increasing the impact resistance of a polymer matrix and are usable as so-called impact modifiers.

The carboxyl-terminated polymers of the formula (II) and end group-terminated polymers of the formula (XV), especially epoxy-terminated polymers of the formula (I), amine-terminated polymers of the formula (XI), (XI′) or (XI″) and (meth)acrylate-terminated polymers of the formula (XII) or (XII′), are preferably liquid or viscous to highly viscous at room temperature. They are preferably processible by the customary means at least at a temperature of 60° C. Most preferably, they are pourable or at least of honeylike consistency at least at 60° C. If they are highly viscous or solid, they can optionally be dissolved, emulsified or dispersed in solvents or resins, such as liquid epoxy resins.

These polymers of the formulae (I), (II), (XI), (XI′), (XI″), (XII) and (XII′) are preferably used in crosslinking compositions, especially in systems into which these polymers can be incorporated by reaction. The question as to the compositions in which these polymers are used thus depends especially on the polymer matrix. For instance, preference is given to using (meth)acrylate-terminated polymers of the formula (XII) or (XII′) especially in (meth)acrylates or unsaturated polyester resins which crosslink to a polymer matrix by means of a free-radically initiated or UV light-initiated polymerization reaction.

Epoxy-terminated polymers of the formula (I) and carboxyl-terminated polymers of the formula (II) and amine-terminated polymers of the formula (XI), (XI′) or (XI″) are preferably used in epoxy resin compositions.

In the case of the epoxy-terminated polymers of the formula (I), they are preferably used in the component in which an epoxy resin A is present. The epoxy resin A may be a liquid epoxy resin of the formula (IX) or a solid epoxy resin of the formula (VIII). In one embodiment, the composition comprises, as well as an epoxy resin A, a hardener B for epoxy resins, which is activated by elevated temperature. Such compositions are used especially as heat-curing epoxy resin adhesives and cure in the course of heating to a temperature above the heat activation of the thermally activable hardener B, so as to form a cured composition.

In the case of the carboxyl-terminated polymers of the formula (II), they can likewise be used in the component in which an epoxy resin A is present.

In the case of the carboxyl-terminated polymers of the formula (II) or of the amine-terminated polymers of the formula (XI), (XI′) or (XI″), they can, however, also be used in a hardener component. Such a hardener component comprises a hardener for epoxy resins, for example polyamines or polymercaptans. As a result of the mixing of the two components, they react with one another, especially also at room temperature, to form a cured composition.

Such compositions can be employed widely. Examples thereof are adhesives, sealants, coatings, foams, structural foams, paints, injection resins or coverings. They can be used, for example, in construction or civil engineering, in the manufacture or repair of industrial goods or consumer goods. They are especially preferably used as adhesives, especially for bodywork construction and the manufacture of windows, domestic appliances or modes of transport, such as water or land vehicles, preferably automobiles, buses, trucks, trains or ships; or as a sealant for sealing joints, seams or cavities in industrial manufacture or repair.

Especially preferably, such compositions are used as crash-resistant adhesives, especially for the construction of modes of transport, preferably in the OEM sector of construction of modes of transport.

Additionally preferably, such compositions are used as structural adhesives for construction and civil engineering, or as highly stressable industrial coatings.

EXAMPLES

Raw materials used

-   Hycar® CTBN 1300×13: acid number=32 mg/g KOH=570 meq/kg     -   Mw=approx. 3150 g/mol -   Epilox F-17-00 (bisphenol F diglycidyl ether=“BFDGE”): 5.88 eq/kg     -   Mw=approx. 170 g/eq -   1,6-Hexanediol: Mw=118.17 g/mol -   Bisphenol A: Mw=228.3 g/mol     Preparation of Carboxyl-Terminated Polymers

Pre-Extended with Hexanediol (“CTBN-HD-CTBN”)

300.0 g (171 meq of COOH) of carboxyl-terminated acrylo-nitrile/butadiene copolymer (Hycar® CTBN 1300×13), 2.53 g of 1,6-hexanediol (42.8 meq of OH) and 1.0 g of p-toluenesulfonic acid monohydrate (5.3 meq) were weighed into a flanged flask with stirrer, nitrogen inlet and vacuum connection. The mixture was stirred to constant weight under gentle vacuum at 150° C. over 4 h. A viscous mass was thus obtained with an acid number of about 23.7 mg/g KOH (approx. 422 meq/kg). The catalyst was not neutralized. The product thus obtained was designated CTBN1.

Preparation of Epoxy-Terminated Polymers

Terminated with BFDGE (“BFDGE-CTBN-HD-CTBN-BFDGE”)

100.0 g (approx. 42.2 meq of COOH) of CTBN1 and 150.0 g (882 meq of epoxy) of Epilox F 17-00 were weighed into a flanged flask with stirrer, nitrogen inlet and vacuum connection. The mixture was stirred under gentle vacuum at 180° C. over 3 h until a viscous epoxy resin with an epoxide content of approx. 3.36 eq/kg was obtained. The product thus obtained was designated ETBN1.

ETBN1 post-extended with bisphenol A (“BFDGE-CTBN-HD-CTBN-BFDGE-BPA-BFDGE-CTBN-HD-CTBN-BFDGE”)

150.0 g (approx. 503 meq of epoxy) of ETBN1 and 7.5 g (approx. 66 meq of OH) of bisphenol A were weighed into a flanged flask with stirrer, nitrogen inlet and vacuum connection. The mixture was stirred under gentle vacuum at 180° C. over 3 h until a viscous epoxy resin with an epoxide content of approx. 2.77 eq/kg was obtained. The product thus obtained was designated ETBN2.

BADGE-Terminated CTBN (Comparison) (“BADGE-CTBN-BADGE”)

100.0 g (approx. 57 meq of COOH) of carboxyl-terminated acrylo-nitrile/butadiene copolymer (Hycar® CTBN 1300×13) and 150.0 g (810 meq of EP) of D.E.R. 331 were weighed into a flanged flask with stirrer, nitrogen inlet and vacuum connection. The mixture was stirred under gentle vacuum at 180° C. over 3 h until a viscous epoxy resin with an epoxide content of approx. 2.99 eq/kg was obtained. The product thus obtained was designated Ref.ETBN.

Efficacy as Impact Modifiers

The epoxy-terminated polymers ETBN1 and ETBN2 exhibited, in heat-curing epoxy resin adhesives, a marked increase in impact resistance compared to the comparative polymer Ref.ETBN.

Illustrative Compositions

The adhesive compositions Z1 and Z2 and the comparative composition ZRef1 according to table 1 were prepared as follows:

A planetary mixer is initially charged with all components apart from dicyandiamide and stirred at 90-100° C. under reduced pressure for one hour, then dicyandiamide is added and, after stirring for a further 10 minutes, the mixtures is transferred to cartridges.

Preparation of a PU Prepolymer PUPrep

150 g of Poly-THF 2000 (BASF, OH number 57 mg/g KOH) and 150 Liquiflex H (Krahn, hydroxyl-terminated polybutadiene, OH number 46 mg/g KOH) were dried at 105° C. under reduced pressure for 30 minutes. Once the temperature had been reduced to 90° C., 61.5 g of isophorone diisocyanate and 0.14 g of dibutyltin dilaurate were added. The reaction was conducted at 90° C. under reduced pressure until the NCO content had become constant at 3.10% after 2.0 h (calculated NCO content: 3.15%). Subsequently, 96.1 g of cardanol (Cardolite NC-700, Cardolite) were added as a blocking agent. The mixture was stirred further at 105° C. under reduced pressure until the NCO content had fallen below 0.1% after 3.5 h. The product was used thus as PUPrep.

Test Methods:

Tensile Strength (TS) (DIN EN ISO 527)

A sample of the composition was pressed to a layer thickness of 2 mm between two Teflon papers. Subsequently, the composition was cured at 180° C. over 30 minutes. The Teflon papers were removed and the specimens were punched according to the DIN standard in the hot state. After storage for 1 day, the test specimens were analyzed under standard climatic conditions with a pulling speed of 2 mm/min.

The tensile strength (“TS”) was determined to DIN EN ISO 527.

Dynamic Resistance to Cleavage (ISO 11343)

The specimens were produced from the compositions described and with electrolytically galvanized DC04 steel (eloZn) with the dimensions 90×20 x 0.8 mm; the adhesive area was 20×30 mm at a layer thickness of 0.3 mm. Curing was effected at 180° C. for 30 min. The dynamic resistance to cleavage was measured in each case at room temperature and at minus 30° C. The impact speed was 2 m/s. The fracture energy (FE) in Joules reported is the area under the measurement curve (from 25% to 90%, to ISO 11343).

TABLE 1 Compositions comprising impact modifiers and test results. ZRef1 Z1 Z2 Araldite ® GT 7071 [PW*] 9 9 9 BADGE [PW*] 26 26 26 Polypox R7 3.0 3.0 3.0 (tert-butylphenyl glycidyl ether, UPPC) [PW*] Ref. ETBN [PW*] 15.0 ETBN1 [PW*] 15.0 ETBN2 [PW*] 15.0 PUPrep [PW*] 15.0 15.0 15.0 Dicyandiamide [PW*] 3.2 3.2 3.2 Aerosil ® R 202 (Degussa) [PW*] 7.0 7.0 7.0 Filler mixture [PW*] 13.0 13.0 13.0 TS [MPa] 31.9 32.3 35.8 FE at 23° C. [J] 17.2 18.8 17.8 FE at −30° C. [J] 4.4 5.4 3.8 *PW = parts by weight. 

1. An epoxy-terminated polymer of the formula (I)

where R¹ is a divalent radical of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN after removal of the terminal carboxyl groups; R² is a radical of a polyol P which has n OH groups, after removal of n OH groups; R³ is a diglycidyl ether DGE after removal of the two glycidyl ether groups; Y¹ is H or methyl; and n is 2 to
 4. 2. The epoxy-terminated polymer as claimed in claim 1, wherein R¹ has the formula (IV)

where the broken lines represent the attachment sites of the two carboxyl groups; b and c are the structural elements which originate from butadiene, and a is the structural element which originates from acrylonitrile; R is a linear or branched alkylene radical having 1 to 6 carbon atoms, which is optionally substituted by unsaturated groups; q is 40 to 100; x =0.05 -0.3, m =0.5-0.8, p =0.1-0.2; with the proviso that x +m +p =1.
 3. The epoxy-terminated polymer as claimed in claim 1, wherein R² is a divalent aliphatic, cycloaliphatic or aromatic organic radical which optionally has oxygen, nitrogen or sulfur atoms.
 4. The epoxy-terminated polymer as claimed in claim 1, wherein the polyol P is a polyoxyalkylenediol.
 5. The epoxy-terminated polymer as claimed in claim 1, wherein R³ has the formula (VI) or (VI′)

where R′, R″ and R′″ are each independently H, methyl or ethyl, z is 0 or 1 and s is 0 or 0.1-12.
 6. The epoxy-terminated polymer as claimed in claim 1, wherein the diglycidyl ether DGE is bisphenol F diglycidyl ether.
 7. The epoxy-terminated polymer as claimed in claim 1, wherein the diglycidyl ether DGE is an aliphatic or cycloaliphatic diglycidyl ether.
 8. The epoxy-terminated polymer as claimed in claim 7, wherein the diglycidyl ether DGE is ethylene glycol diglycidyl ether, butanediol diglycidyl ether or hexanediol diglycidyl ether.
 9. A carboxyl-terminated polymer of the formula (II)

where R¹ is a divalent radical of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN after removal of the terminal carboxyl groups; R² is a radical of a polyol P which has n OH groups, after removal of n OH groups; and n is 2 to
 4. 10. The carboxyl-terminated polymer as claimed in claim 9, wherein R¹ has the formula (IV)

where the broken lines represent the attachment sites of the two carboxyl groups; b and c are the structural elements which originate from butadiene, and a is the structural element which originates from acrylonitrile; R is a linear or branched alkylene radical having 1 to 6 carbon atoms, which is optionally substituted by unsaturated groups; q is 40 to 100; x =0.05-0.3, m =0.5-0.8, p =0.1-0.2; with the proviso that x +m +p =1.
 11. An amine-terminated polymer of the formula (XI) or (XI′) or (XI″)

where R¹ is a divalent radical of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN after removal of the terminal carboxyl groups; R² is a radical of a polyol P which has n OH groups, after removal of n OH groups; and n is 2 to
 4. 12. A (meth)acrylate-terminated polymer of the formula (XII) or (XII′)

where R¹ is a divalent radical of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN after removal of the terminal carboxyl groups; R² is a radical of a polyol P which has n OH groups n OH groups; R⁷ is H or methyl; R⁸ is a divalent radical, and n is 2 to
 4. 13. A process for preparing a carboxyl-terminated polymer as claimed in claim 9 by a reaction of a polyol P of the formula R²(OH)_(n) with a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN of the formula HOOC—R¹—COOH, wherein R²(OH)_(n) and HOOC—R¹—COOH are used for this reaction in an amount relative to one another which corresponds to a stoichiometric ratio of the COOH groups to OH groups [COOH]/[OH] of≧2.
 14. A process for preparing an epoxy-terminated polymer as claimed in claim 1 by a reaction of a carboxyl-terminated polymer of the formula (II)

where R1 is a divalent radical of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN after removal of the terminal carboxyl groups; R2 is a radical of a polyol P which has n OH groups, after removal of n OH groups; n is 2 to 4, with a diglycidyl ether of the formula (III),

wherein the polymer of the formula (II) and the diglycidyl ether of the formula (III) are used for this reaction in an amount relative to one another which corresponds to a stoichiometric ratio of the glycidyl ether groups to COOH groups

of≧2.
 15. A process for preparing an end group-terminated polymer of the formula (XV)

comprising the following two steps: a) pre-extension, i.e. reaction of a polyol P of the formula R²(OH)_(n) with a stoichiometric excess of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN of the formula HOOC—R¹—COOH to give a carboxyl-terminated polymer of the formula (II) as claimed in claim 9, in such a way that the polyol P and HOOC-R¹-COOH are used in an amount relative to one another such that the ratio of COOH groups to OH groups [COOH]/[OH] is≧2; where R¹ is a divalent radical of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN after removal of the terminal carboxyl groups; R² is a radical of a polyol P which has n OH groups, after removal of n OH groups; and b) termination, i.e. reacting a carboxyl-terminated polymer of the formula (II) with a diglycidyl ether or with a diamine or with a (meth)acrylate-functional alcohol or with a glycidyl ether-functional (meth)acrylate in such a way that the diglycidyl ether or the diamine or the (meth)acrylate-functional alcohol or the glycidyl ether-functional (meth)acrylate and the carboxyl-terminated polymer of the formula (II) are used in an amount relative to one another which corresponds to one molecule of diglycidyl ether or diamine or (meth)acrylate-functional alcohol or glycidyl ether-functional (meth)acrylate per COOH group of a molecule of carboxyl-terminated polymer of the formula (II); where, in formula (XV), R¹⁰ is a divalent radical and Q¹ is an end group which is selected from the group consisting of the formulae (XVI), (XVI′), (XVI″) and —NH₂

with the proviso that Q is —NH— in the case in which Q¹ is —NH₂ or the formula (XVI″), and Q is —O— or the formula (XVII) in the case in which Q¹ is the formula (XVI′), and Q is the formula (XVII) in the case in which Q¹ is the formula (XVI).
 16. A method of increasing the impact resistance of a polymer matrix, comprising: providing a carboxyl-terminated polymer of the formula (II);

where R¹ is a divalent radical of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN after removal of the terminal carboxyl groups, R² is a radical of a polyol P which has n OH groups, after removal of n OH groups, and n is 2 to 4; and preparing an end group-terminated polymer of the formula (XV) by the process as claimed in claim
 15. 17. The method as claimed in claim 16, wherein the polymer matrix is an epoxy resin matrix.
 18. A composition comprising an amine-terminated polymer of the formula (XI) or (XI′) or (XI″) as claimed in claim 11 or a (meth)acrylate-terminated polymer of the formula (XII) or (XII′)

where R¹ is a divalent radical of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN after removal of the terminal carboxyl groups, R² is a radical of a polyol P which has n OH groups n OH groups, R⁷ is H or methyl, R⁸ is a divalent radical, and n is 2 to
 4. 19. A composition comprising an epoxy-terminated polymer of the formula (I) as claimed in claim 1 or a carboxyl-terminated polymer of the formula (II),

where R¹ is a divalent radical of a carboxyl-terminated butadiene/acrylonitrile copolymer CTBN after removal of the terminal carboxyl groups, R² is a radical of a polyol P which has n OH groups, after removal of n OH groups, and n is 2 to
 4. 20. The composition as claimed in claim 19, wherein the composition further comprises at least one epoxy resin A.
 21. The composition as claimed in claim 20, wherein the composition further comprises a hardener B for epoxy resins, which is activated by elevated temperature.
 22. A cured composition obtained from a composition as claimed in claim 20, further comprising of a hardener for epoxy resins.
 23. A cured composition obtained from heating a composition as claimed in claim 21 to a temperature above the heat activation of the thermally activable hardener B. 